| Literature DB >> 31736872 |
Abstract
In the beginning of the twenty first century, the International Program on Chemical Safety published a document entitled Global Assessment of the State-Of-The-Science of Endocrine Disruptors. The work indicated only weak evidence of endocrine-related effects in human populations, and in wild animal populations. This document was revised in 2012 (State of the Science of Endocrine Disrupting Chemicals-2012) (1). The new document and the extensive scientific evidence it provided showed clearly that ED effects could be a risk to human and wildlife health. These works, however, were focused in human health and related animal models, mainly vertebrates and particularly mammals. It can be argued that invertebrates and many other taxa are important parts of all ecosystems, and, in many instances, have been shown to be also vulnerable to endocrine disruption. Thus, this work is aimed to show some observations on important marine invertebrate taxa, from an ecological point of view. The most important example of endocrine disruption in marine wild populations is the imposex response of marine gastropods, known for more than 40 years, and worldwide used to evaluate marine antifouling pollution. Among the mollusks, other important natural resources are bivalve species, used as human food sources and cephalopods, free-living, highly specialized mollusks, and also human food sources. Effects derived from endocrine disruptors in these species indicate that consumption could bring these compounds to human populations in an almost direct way, sometimes without any form of cooking or preparation. While discussing these questions, this work is also aimed to stimulate research on endocrine disruption among the invertebrate taxa that inhabited our oceans, and on which these effects are poorly known today.Entities:
Keywords: ecological risk assessment; endocrine disruption; environmental pollution; marine invertebrates; reproduction
Year: 2019 PMID: 31736872 PMCID: PMC6828821 DOI: 10.3389/fendo.2019.00721
Source DB: PubMed Journal: Front Endocrinol (Lausanne) ISSN: 1664-2392 Impact factor: 5.555
Some examples of endocrine disrupting compounds and their range of effects in marine invertebrate species.
| TBT, DBT | Lower progesterone levels, sexual maturation delay, “F” | ( | |
| TBT | Skewed sex ratio, vitellin reduction, oestradiol-17β production in gonad reduced “F” | ( | |
| TBT | Increase in testosterone, oestradiol decrease “F” | ( | |
| TBT | Intersexuality, ovary spermatogenesis, “F” | ( | |
| North Sea Oil (NSO) | Ovarian follicle development, normal spermatogenesis | ( | |
| NSO + PAH + Alkylphenols | Male gonadal melanomacrophage centers, degeneration ovary follicles | ( | |
| Bisphenol A | Spawning induction for both sexes, ovocyte atresia | ( | |
| 2,2′,4,4′-tetrabromodiphenyl ether | Ovocyte atresia, male spawning induction | ( | |
| Diallyl phthalate | Follicle and ovocyte reduction, male spawning induction | ( | |
| PAHs, TBT | Intersexuality, oocite atresia “F” | ( | |
| Benzo(a)pyrene | Reduced ovarian growth, testosterone, progesterone and 17βestradiol secretion reduction | ( | |
| Benzo(a)pyrene | Reduced testosterone and 17βestradiol production, progesterone disruption in ovary, ovarian impairment, development delay | ( | |
| Bisphenol A, 17βestradiol | Gene transcription | ( | |
| Testosterone | Increased swimming, fertilization rate and recognition ability in males | ( | |
| Progesterone, flutamide (non-steroidal anti-androgen) | Inhibited swimming speed, suppression of fertilization and reduced recognition ability in males | ( | |
| Dibutyl phthalate | Sperm dysfunction, impaired embryogenesis | ( | |
| Propylparaben | Sex ratio alteration toward females | ( |
Most were laboratory studies, while those including field studies are indicated by the letter “F.” Bold letters, population reduction observed.
Figure 1Imposex development is different marine gastropod species at increasing water TBT concentrations. Imposex intensity: values of VDSI index measured for each species; TBT water concentrations in ng(Sn). L−1. Ecological risk indicated by light gray bars indicating population damage by lack of recruitment due to female sterility. Vertical concentration lines: A: TBT EQS of the UK; B: Brazilian limit for sea waters, Class 1, CONAMA Resolution 357. Modified from Stroben et al. (44) by the author.
Figure 2Evolution of the marine gastropod Stramonita brasiliensis populations at Guanabara Bay, Brazil, between 1960 and 2013. Organotin sources and expression of imposex development are also shown. Modified from Toste et al. (45).
Figure 3Imposex development scheme for Stramonita brasiliana (Stramonita haemastoma as originally published) with high and low exposition routes, according to Toste et al. (45). Captions: te, tentacle; pp, penis primordium; gp, genital papilla; vds, vas deferens; ov, obstructed vulva; ac, aborted capsules. The inclination of the routes at the same stages is related to relative organotins exposition: the nearer to stage 1, lower expositions were indicated by distance for organotins sources in the field. Dark arrows indicate the more commonly observed routes in Southeastern Brazil.
Figure 4(A) Schematic scheme for an interference mechanism in the imposex response of marine gastropod mollusk to organotin compounds. While cationic organotins are the most available form to biota, both particulate and dissolved organic matter from sewage can complex organotins, while sewage is also a source of xenoestrogens that may act as antagonists to imposex development. (B) Main environmental aspects of the interference mechanism proposed. Due to the multiple variables involved, only the general lines are indicated.